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【结 构 式】

【分子编号】66561

【品名】3-(2-chloroethyl)-9-hydroxy-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one

【CA登记号】130049-82-0

【 分 子 式 】C11H15ClN2O2

【 分 子 量 】242.70508

【元素组成】C 54.44% H 6.23% Cl 14.61% N 11.54% O 13.18%

与该中间体有关的原料药合成路线共 2 条

合成路线1

该中间体在本合成路线中的序号:(III)

 

1 Janssen CGM,Knaeps AG.Kennis LE.et aL 1989. Novel 3-piperidinyl-1,2-benzisoxazoles, EP 0368388
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 37087 3-(benzyloxy)-2-pyridinylamine; 3-(benzyloxy)-2-pyridinamine 24016-03-3 C12H12N2O 详情 详情
(II) 66560 3-(2-Chloroethyl)-2-methyl-9-benzyloxy-4H-pyrido[1,2-a]pyrimidin-4-one;9-Benzyloxy-3-(2-chloroethyl)-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one 147687-17-0 C18H17ClN2O2 详情 详情
(III) 66561 3-(2-chloroethyl)-9-hydroxy-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one 130049-82-0 C11H15ClN2O2 详情 详情
(IV) 66562 6-fluoro-3-(piperidin-4-yl)-3a,4,5,6,7,7a-hexahydrobenzo[d]isoxazole   C12H19FN2O 详情 详情

合成路线2

该中间体在本合成路线中的序号:(II)

 

1 Smet KD, Dun JV, Stokbroekx B.et aL 2005. Selectivity gontrol by use of near-IR for a hydrogenation process. Org Proc Res Dev,9: 344一347
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 66563 3-(2-chloroethyl)-9-hydroxy-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one   C11H11ClN2O2 详情 详情
(II) 66561 3-(2-chloroethyl)-9-hydroxy-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one 130049-82-0 C11H15ClN2O2 详情 详情
(III) 66564 9-hydroxy-2-methyl-3-propyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one   C12H18N2O2 详情 详情
(IV) 23044 3-(2-chloroethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one 63234-80-0 C11H15ClN2O 详情 详情
(V) 66565 3-(2-chloroethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one   C11H16N2O3 详情 详情
(VI) 66566 3-ethyl-9-hydroxy-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one   C11H12N2O2 详情 详情
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